COREGA TABLETS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign report with the FDA on 2019-05-29 for COREGA TABLETS manufactured by Block Drug Co., Inc..

Event Text Entries

[146355814] Argus case (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[146355815] Inappropriate usage [accidental device ingestion]. Case description: this case was reported by a consumer via call center representative and described the occurrence of accidental device ingestion in a female patient who received denture cleanser (corega tablets) tablet for product used for unknown indication. On an unknown date, the patient started corega tablets at an unknown dose and frequency. On an unknown date, an unknown time after starting corega tablets, the patient experienced accidental device ingestion (serious criteria gsk medically significant). Corega tablets was discontinued. On an unknown date, the outcome of the accidental device ingestion was recovered/resolved. It was unknown if the reporter considered the accidental device ingestion to be related to corega tablets. Additional details: this case received from turkey regulatory authority. Corega denture cleanser drunk by the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020379-2019-00031
MDR Report Key8649392
Report SourceCONSUMER,FOREIGN
Date Received2019-05-29
Date of Report2019-05-14
Date Mfgr Received2019-05-14
Date Added to Maude2019-05-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer StreetPO BOX 13398 RESEARCH TRIANGLE PARK
Manufacturer CityNC 27709
Manufacturer CountryUS
Manufacturer Postal27709
Manufacturer Phone8888255249
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOREGA TABLETS
Generic NameDENTURE CLEANSER
Product CodeEFT
Date Received2019-05-29
OperatorLAY USER/PATIENT
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBLOCK DRUG CO., INC.
Manufacturer AddressMEMPHIS TN US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-05-29

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